BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Remington Medical, Inc.

    Reg #: 3007014520 · FEI: 3007014520 · Expires 2026
    View on FDA
    Products
    38
    Proprietary Names
    32
    Establishment Types
    3
    Classifications
    38

    Registration Details

    Registration Name
    Remington Medical, Inc.
    Registration Number
    3007014520
    FEI Number
    3007014520
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    6245 Shiloh Road, Suite C
    City
    Alpharetta
    State
    GA
    ZIP
    30005
    Country
    US

    Regulatory Submissions

    510(k) Number
    K983621

    Owner / Operator

    Firm Name
    REMINGTON MEDICAL, INC.
    Operator Number
    9006473
    Address
    6830 MEADOWRIDGE CT., --
    City
    Alpharetta
    State
    GA
    Postal Code
    30005
    Country
    US

    Products

    Device Name Product Code
    Stimulator, Electrical, Evoked Response GWF
    Neurological Stereotaxic Instrument HAW
    System, X-Ray, Mammographic IZH
    Orthopedic Stereotaxic Instrument OLO
    Eyelid Thermal Pulsation System ORZ
    Stimulator, Nerve ETN
    Intervertebral Fusion Device With Bone Graft, Thoracic PHM
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX
    Table, Operating-Room, Ac-Powered FQO
    Tape And Bandage, Adhesive KGX
    Catheter, Steerable DRA
    Marker, Skin FZZ
    Neurosurgical Nerve Locator PDQ
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Thoracolumbosacral Pedicle Screw System NKB
    Flowmeter, Blood, Cardiovascular DPW
    Instrument, Ultrasonic Surgical LFL
    Spinal Vertebral Body Replacement Device - Cervical PLR
    Appliance, Fixation, Spinal Interlaminal KWP
    Dispenser, Liquid Medication KYX
    Tubes, Gastrointestinal (And Accessories) KNT
    Cable, Electrode IKD
    Cuff, Tracheal Tube, Inflatable BSK
    Retractor, Fiberoptic FDG
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Cable, Transducer And Electrode, Patient, (Including Connector) DSA
    Instrument, Biopsy KNW
    Caliper, Ophthalmic HOE
    Orthopedic Manual Surgical Instrument LXH
    Electromyograph, Diagnostic IKN
    Clamp, Vascular DXC
    Bit, Drill HTW
    Endoscope Channel Accessory ODC
    Skin Patch For Treatment Of Hyperhidrosis QVX
    Bone Cement, Posterior Screw Augmentation PML
    Orthosis, Spinal Pedicle Fixation MNI
    Orthosis, Spondylolisthesis Spinal Fixation MNH
    Set, I.V. Fluid Transfer LHI

    Proprietary Names

    LNGC-14 LNGO-2022 LNGC-2022 Pneumatic Button Cable Myelotec Video Guided Steerable Catheter VascuChek Transceiver VascuChek Clinical Probe VascuChek Charger VascuChek Kit VascuChek System TendoNova Ocelot TDS 1000 Adapter Cap Bionix Internal Feeding Tube Declogger McKesson Internal Feeding Tube Declogger VascuChek ADAP-1 Family FL-601-97 Family BS-101-97 Family ADAP-2R Family PA-801 Family 301-CG Family ADAP-2000 Family ADAP-2RL Family S-201-97 Family ADAP-2 Family S-101-97 Family FL-II Family Graft Delivery Sleeves and Caps, Sterile Kit N-SWEAT SweatTech Brella®, 3-minute patch, axilla VascuChek Surgical Probe

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device Manufacture Device in the United States for Export Only